Evidence map›Paper›PMID 22966003›Full record

ArticleThe Journal of experimental medicine2012

Neuropilin-1 distinguishes natural and inducible regulatory T cells among regulatory T cell subsets in vivo.

Mahesh Yadav, Cedric Louvet, Dan Davini, James M Gardner, Marc Martinez-Llordella, Samantha Bailey-Bucktrout, Bryan A Anthony, Francis M Sverdrup, Richard Head, Daniel J Kuster and 4 more

Abstract read
In one paragraph

Article in The Journal of experimental medicine, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 402 papers.

0numbers the graph read from it
0cells of the map it votes in
402citing papers in PubMed
26.4field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

402 citing papers in PubMed, 625 citations in OpenAlex.

  1. Regulatory T cells in the skin: Origin, function, and plasticity.JID innovations : skin science from molecules to population health · 2026
    Review
  2. Review
  3. Regulatory T cells in cancer and inflammation.Signal transduction and targeted therapy · 2026
    Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Immunomodulation by allograft endothelial cells.Frontiers in transplantation · 2025
    Review

342 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 4 institutions in 2 countries.

Mahesh YadavDiabetes Center, University of California, San Francisco, San Francisco, CA 94122, USA.
Cedric Louvet
Dan Davini
James M Gardner
Marc Martinez-Llordella
Samantha Bailey-Bucktrout
Bryan A Anthony
Francis M Sverdrup
Richard Head
Daniel J Kuster
Peter Ruminski
David Weiss
David Von Schack
Jeffrey A Bluestone
Pfizer (United States) · USDiabetes Australia · AUUniversity of California, San Francisco · USSaint Louis University · US

Funding

Research BaseP30DK063720 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI VAISSE, CHRISTIAN · 2003 to 2019
$21.8M
Spontaneous Autoimmune Model of Peripheral NeuropathyR01AI050834 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BLUESTONE, JEFFREY A · 2002 to 2011
$3.1M
IMMUNOMODULATION OF TRANSPLANT REJECTION BY ANTI-CD3 MABR01AI046643 · NIAID · UNIVERSITY OF CHICAGO · PI BLUESTONE, JEFFREY A · 2000 to 2015
$1.8M
NIAID NIH HHS R01 AI046643NIAID NIH HHS R01 AI050834NIAID NIH HHS R01 AI50834NIDDK NIH HHS P30 DK063720NIDDK NIH HHS P30DK63720
6 · The paper itself

Abstract

Foxp3(+) CD4(+) T helper cells called regulatory T (T reg) cells play a key role in controlling reactivity to self-antigens and onset of autoimmunity. T reg cells either arise in thymus and are called natural T reg (nT reg) cells or are generated in the periphery through induction of Foxp3 and are called inducible T reg (iT reg) cells. The relative contributions of iT reg cells and nT reg cells in peripheral tolerance remain unclear as a result of an inability to separate these two subsets of T reg cells. Using a combination of novel TCR transgenic mice with a defined self-antigen specificity and conventional mouse models, we demonstrate that a cell surface molecule, neuropilin-1 (Nrp-1), is expressed at high levels on nT reg cells and can be used to separate nT reg versus iT reg cells in certain physiological settings. In addition, iT reg cells generated through antigen delivery or converted under homeostatic conditions lack Nrp-1 expression. Nrp-1(lo) iT reg cells show similar suppressive activity to nT reg cells in controlling ongoing autoimmune responses under homeostatic conditions. In contrast, their activity might be compromised in certain lymphopenic settings. Collectively, our data show that Nrp-1 provides an excellent marker to distinguish distinct T reg subsets and will be useful in studying the role of nT reg versus iT reg cells in different disease settings.

Indexed as

AnimalsAutoimmunityGene Expression RegulationLymphocyte ActivationLymphoid TissueMaleMiceMice, Inbred C57BLMice, Inbred NODMice, TransgenicMyelin Basic ProteinNeuropilin-1Receptors, Antigen, T-CellT-Lymphocytes, RegulatoryT-Lymphocyte SubsetsMyelin Basic ProteinNeuropilin-1Receptors, Antigen, T-Cell

Identifiers

PMID22966003
PMCPMC3457729
OpenAlexW2112498628

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.